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J R Eckman

Showing results (11-20 of 27) with videos related to

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Pediatrics|March 1, 1994
Comparison of liquid and dried blood for neonatal hemoglobinopathy screening: laboratory and programmatic issuesC Papadea, J R Eckman, R S Kuehnert, et al.
Blood|May 15, 1995
Double-stranded RNA induces sickle erythrocyte adherence to endothelium: a potential role for viral infection in vaso-occlusive pain episodes in sickle cell anemiaP A Smolinski, M K Offermann, J R Eckman, et al.
The Journal of Bone and Joint Surgery. American Volume|July 1, 1988
Total hip arthroplasty in patients who have sickle-cell hemoglobinopathyA R Bishop, J R Roberson, J R Eckman, et al.
Blood|September 15, 1993
Alpha 4 beta 1-integrin expression on sickle reticulocytes: vascular cell adhesion molecule-1-dependent binding to endotheliumR A Swerlick, J R Eckman, A Kumar, et al.
The Journal of Laboratory and Clinical Medicine|October 1, 1977
Host heme catabolism in drug-sensitive and drug-resistant malariaJ R Eckman, S Modler, J W Eaton, et al.
Journal of Pediatric Psychology|November 24, 1998
Family functioning and social support in the adaptation of caregivers of children with sickle cell syndromesC E Ievers, R T Brown, R G Lambert, et al.
Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists|January 1, 1994
Sustained attention and inhibitory control in children with sickle cell syndromeB T Goonan, L J Goonan, R T Brown, et al.
Blood|April 15, 1993
Thrombospondin from activated platelets promotes sickle erythrocyte adherence to human microvascular endothelium under physiologic flow: a potential role for platelet activation in sickle cell vaso-occlusionH A Brittain, J R Eckman, R A Swerlick, et al.
Thrombosis and Haemostasis|July 4, 2001
Reduction of pain episodes and prothrombotic activity in sickle cell disease by dietary n-3 fatty acidsA Tomer, S Kasey, W E Connor, et al.
Journal of the American Society of Nephrology : JASN|May 8, 1999
Evidence that microdeletions in the alpha globin gene protect against the development of sickle cell glomerulopathy in humansA Guasch, C F Zayas, J R Eckman, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Pediatrics|March 1, 1994
Comparison of liquid and dried blood for neonatal hemoglobinopathy screening: laboratory and programmatic issuesC Papadea, J R Eckman, R S Kuehnert, et al.
Blood|May 15, 1995
Double-stranded RNA induces sickle erythrocyte adherence to endothelium: a potential role for viral infection in vaso-occlusive pain episodes in sickle cell anemiaP A Smolinski, M K Offermann, J R Eckman, et al.
The Journal of Bone and Joint Surgery. American Volume|July 1, 1988
Total hip arthroplasty in patients who have sickle-cell hemoglobinopathyA R Bishop, J R Roberson, J R Eckman, et al.
Blood|September 15, 1993
Alpha 4 beta 1-integrin expression on sickle reticulocytes: vascular cell adhesion molecule-1-dependent binding to endotheliumR A Swerlick, J R Eckman, A Kumar, et al.
The Journal of Laboratory and Clinical Medicine|October 1, 1977
Host heme catabolism in drug-sensitive and drug-resistant malariaJ R Eckman, S Modler, J W Eaton, et al.
Journal of Pediatric Psychology|November 24, 1998
Family functioning and social support in the adaptation of caregivers of children with sickle cell syndromesC E Ievers, R T Brown, R G Lambert, et al.
Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists|January 1, 1994
Sustained attention and inhibitory control in children with sickle cell syndromeB T Goonan, L J Goonan, R T Brown, et al.
Blood|April 15, 1993
Thrombospondin from activated platelets promotes sickle erythrocyte adherence to human microvascular endothelium under physiologic flow: a potential role for platelet activation in sickle cell vaso-occlusionH A Brittain, J R Eckman, R A Swerlick, et al.
Thrombosis and Haemostasis|July 4, 2001
Reduction of pain episodes and prothrombotic activity in sickle cell disease by dietary n-3 fatty acidsA Tomer, S Kasey, W E Connor, et al.
Journal of the American Society of Nephrology : JASN|May 8, 1999
Evidence that microdeletions in the alpha globin gene protect against the development of sickle cell glomerulopathy in humansA Guasch, C F Zayas, J R Eckman, et al.
Pageof 3